Medtronic Recalls Certain Newport Ventilators and Related Service Parts
Customers are being asked to remove the affected devices from use and replace with an alternate means of ventilation.
Customers are being asked to remove the affected devices from use and replace with an alternate means of ventilation.
BD is correcting software for its Alaris Systems Manager and CCE Infusion Adapter after identifying a risk that outdated infusion parameters could be uploaded, potentially leading to incorrect dosing.
Philips’ cardiac telemetry Monitoring Service Application did not route some ECG events from July 2022 to July 2024 for cardiology review.
Customers are being asked to remove the affected devices from use and replace with an alternate means of ventilation.
Baxter is recalling certain Volara System components due to a disconnection issue that may lead to insufficient ventilation.
Read MoreDefibtech is recalling its RMU-2000 ARM XR Chest Compression Devices due to a motor issue that may cause the device to stop compressions, leading to potential patient injury or death.
Read MoreTandem Diabetes Care, Inc. provided an update on the t:connect app due to an issue causing rapid depletion of the tX2 insulin pump battery.
Read MorePhilips has filed a lawsuit against PSN Labs, claiming incorrect analysis of foam material used in recalled ventilation devices.
Read MoreThe U.S. FDA and Health Canada are raising awareness about the safe use of Mega 2000 and Mega Soft Patient Return Electrodes by Megadyne Medical Products, Inc. due to reported burn injuries. Four voluntary recalls have been initiated since June 2023.
Read MoreBaxter is recalling the Life2000 Ventilator System due to potential battery charging dongle failure, which can prevent or hinder charging.
Read MoreHamilton Medical issued a software correction for the Hamilton-C6 ventilator due to a failure to restart ventilation in sensor fail mode.